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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241070Generated: October 31, 2026

Acetone → 4-[(2-Amino-5-bromopyridin-3-yl)sulfinyl]-2-methylbutan-2-ol

https://huagongshe.com/reaction/241070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
ReactantPotassium peroxymonosulphateHCID 10313463—
ReactantHCID 66820470HCID 66820470—
SolventMethanolHCID 887—
Product4-[(2-Amino-5-bromopyridin-3-yl)sulfinyl]-2-methylbutan-2-olHCID 6682059160%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-[(2-amino-5-bromopyridin-3-yl)thio]-2-methylbutan-2-ol (83 mg, 0.28 mmol) in a mixture of methanol (750 μL), acetone (750 μL) and water (450 μL) was added potassium peroxymonosulfate (131 mg, 0.21 mmol) and the reaction mixture was stirred for 90 minutes at 0° C. The reaction mixture was partitioned between water (20 mL) and ethyl acetate (50 mL). The organic layer was separated and washed with water (20 mL) and brine (20 mL), dried over sodium sulfate, filtered and concentrated. Purification by flash chromatography (35% to 80% ethyl acetate in hexane) gave 4-[(2-amino-5-bromopyridin-3-yl)sulfinyl]-2-methylbutan-2-ol (52 mg, 60%); MS (EI) for C10H15BrN2O2S: 308 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648066B2
Source datasetuspto-grants-2014_02
ORD IDord-562c0c0b70344e33823acd6ef6af8784
Source noteuspto-grants-2014_02